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Variant (rsID / SNP)

rs146074150

ALK

rs146074150 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALK. Location: chromosome 2, position 29,446,231. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ALKBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
2:29446231
Cytoband
2p23.2
HGVS
NM_004304.5(ALK):c.3336G>A (p.Pro1112=)
Allele change
Synonymous_P1112P

Associated conditions / phenotypes

Neuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.